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G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes

Solubilization of single walled carbon nanotubes (SWNTs) in aqueous gel phases formed by reversible, G-quadruplex self-assembly of guanosine monophosphate (GMP) alone or with guanosine (Guo) is described. Unlike other media and methods for aqueous solubilization of SWNTs, the guanosine gels (“G-gels...

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Autores principales: Yu, Yuehua, Pushparaj, Victor L., Nalamasu, Omkaram, McGown, Linda B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269963/
https://www.ncbi.nlm.nih.gov/pubmed/24335620
http://dx.doi.org/10.3390/molecules181215434
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author Yu, Yuehua
Pushparaj, Victor L.
Nalamasu, Omkaram
McGown, Linda B.
author_facet Yu, Yuehua
Pushparaj, Victor L.
Nalamasu, Omkaram
McGown, Linda B.
author_sort Yu, Yuehua
collection PubMed
description Solubilization of single walled carbon nanotubes (SWNTs) in aqueous gel phases formed by reversible, G-quadruplex self-assembly of guanosine monophosphate (GMP) alone or with guanosine (Guo) is described. Unlike other media and methods for aqueous solubilization of SWNTs, the guanosine gels (“G-gels”) are found to readily disperse high (>mg/mL) concentrations of individual rather than bundled SWNTs. SWNT dispersions in GMP alone precipitate in several hours and re-form upon shaking; however, dispersions in the binary GMP/Guo gels are indefinitely stable. Increasing GMP or KCl concentration in the binary gels increased the relative abundance of large diameter and semi-conducting SWNTs. Different gel compositions also displayed different selectivities toward SWNTs of different chiralities. These results indicate a strong connection between the self-assembled G-gels and the dimensions and structures of the SWNTs that they solubilize.
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spelling pubmed-62699632018-12-20 G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes Yu, Yuehua Pushparaj, Victor L. Nalamasu, Omkaram McGown, Linda B. Molecules Article Solubilization of single walled carbon nanotubes (SWNTs) in aqueous gel phases formed by reversible, G-quadruplex self-assembly of guanosine monophosphate (GMP) alone or with guanosine (Guo) is described. Unlike other media and methods for aqueous solubilization of SWNTs, the guanosine gels (“G-gels”) are found to readily disperse high (>mg/mL) concentrations of individual rather than bundled SWNTs. SWNT dispersions in GMP alone precipitate in several hours and re-form upon shaking; however, dispersions in the binary GMP/Guo gels are indefinitely stable. Increasing GMP or KCl concentration in the binary gels increased the relative abundance of large diameter and semi-conducting SWNTs. Different gel compositions also displayed different selectivities toward SWNTs of different chiralities. These results indicate a strong connection between the self-assembled G-gels and the dimensions and structures of the SWNTs that they solubilize. MDPI 2013-12-11 /pmc/articles/PMC6269963/ /pubmed/24335620 http://dx.doi.org/10.3390/molecules181215434 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Yu, Yuehua
Pushparaj, Victor L.
Nalamasu, Omkaram
McGown, Linda B.
G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes
title G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes
title_full G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes
title_fullStr G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes
title_full_unstemmed G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes
title_short G-Quadruplex Guanosine Gels and Single Walled Carbon Nanotubes
title_sort g-quadruplex guanosine gels and single walled carbon nanotubes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269963/
https://www.ncbi.nlm.nih.gov/pubmed/24335620
http://dx.doi.org/10.3390/molecules181215434
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